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Structure of 944896-67-7
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Ethyl 6-bromoimidazo[1,2-a]pyrimidine-2-carboxylate features a brominated imidazopyrimidine core that enables direct functionalization in cross-coupling reactions. The ester group enhances solubility and facilitates downstream derivatization. This bench-stable, moisture-tolerant building block integrates readily into heterocyclic scaffolds for medicinal chemistry applications.
Ethyl 6-bromoimidazo[1,2-a]pyrimidine-2-carboxylate serves as a versatile building block for the synthesis of imidazopyrimidine-based scaffolds. The bromine at the C6 position enables palladium-catalyzed cross-coupling reactions, while the ester group facilitates further derivatization. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive heterocycles.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: